Blocking XIAP:CASP7-p19 selectively induces apoptosis of CASP3/DR malignancies by a novel reversible small molecule. [PDF]
Chen SH +8 more
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Monogenic forms of inflammatory bowel disease: Genetic mechanisms, models, and clinical implications. [PDF]
Ghorbanpour A +5 more
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Late presentation of X-linked inhibitor of apoptosis (XIAP) deficiency in a young adult. [PDF]
Nazarali S, Derfalvi B, Clark P.
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LncRNA SNHG4 Regulates Lipid Metabolism and Inflammation in Non-Alcoholic Fatty Liver Disease by Targeting miR-34b-5p/XIAP Axis. [PDF]
Ding Y, Zheng S, Fu XN, Ma C, Juan Y.
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A dual inhibitor of TrxR1 and XIAP induces pyroptosis in melanoma. [PDF]
Wang Y +6 more
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Targeted therapies and their outcomes in monogenic very early onset inflammatory bowel disease: a systematic review. [PDF]
Abhari AP +6 more
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Controlling the activity of caspases is essential for the appropriate execution of cell death and the regulation of cell survival. One cellular inhibitor of apoptosis, XIAP, has emerged as a crucial regulator of caspases, and is itself subject to complex negative regulation.
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Quercetin ameliorates XIAP deficiency–associated hyperinflammation
Blood, 2022Abstract XIAP (X-linked inhibitor of apoptosis) deficiency is a rare inborn error of immunity. XIAP deficiency causes hyperinflammatory disease manifestations due to dysregulated TNF (tumor necrosis factor)-receptor signaling and NLRP3 (NOD- [nucleotide-binding oligomerization domain], LRR- [leucine-rich repeat] and pyrin domain ...
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XIAP deficiency syndrome in humans
Seminars in Cell and Developmental Biology, 2015The X-linked inhibitor of apoptosis (XIAP) deficiency, also known as the X-linked lymphoproliferative syndrome type 2 (XLP-2), is a rare primary immunodeficiency. XIAP deficiency is characterized by a key triad of clinical manisfestations, which consist of a high susceptibility to develop hemophagocytic lymphohistiocytosis (HLH) frequently triggered by
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